Clinical Monitoring

Effective clinical monitoring is vital for the success of a trial and plays a crucial role in accelerating a drug’s market launch.

While the initiation of the first site in a trial marks a significant milestone, the activation of the final site is equally critical, as it maximizes patient recruitment opportunities.

Our team of highly trained, expert, and safety-focused clinical research professionals offers clinical trial monitoring services tailored specifically to your study protocol.

Collaborating closely with site management and study physicians, our clinical monitoring team embodies a patient-centric approach to guide you through every phase of your clinical trial.

Our clinical trial monitoring professionals hold at least an undergraduate degree in life sciences or equivalent education and experience. They bring an average of four years of clinical research experience, covering all phases of trials.

Our clinical trial monitoring experts provide support in the following areas:

• Site Identification and Selection: Conducting on-site or remote pre-study visits.
• Site Initiation, Monitoring, and Close-Out: Managing on-site or remote activities throughout the trial.
• Participant Protection: Ensuring the rights and well-being of trial participants are safeguarded.
• Data Integrity and Safety: Monitoring to confirm consent, eligibility, safety, and data accuracy.
• Site Staff Training: Educating investigational site staff on trial procedures.
• Document Handling: Overseeing informed consent/document translation, verification, and back-translation.
• Regulatory Submissions: Preparing and submitting documents to regulatory or ethics/review boards.
• Protocol Compliance: Ensuring timely submission of protocols, consent forms, and related documents.
• Study Material Management: Handling drug storage, intellectual property, and clinical study materials.
• Protocol Deviation Reporting: Monitoring and reporting any deviations from the protocol.
• Regular Reporting: Providing consistent updates and reports throughout the trial.

Our clinical monitoring team is dedicated to ensuring that every aspect of your trial is conducted with the highest standards of quality and care.